Neuroendocrine Tumors, Version 1.2015

Autor: Martin J. Heslin, Manisha H. Shah, Deborah A. Freedman-Cass, James C. Yao, Paul T. Fanta, Fouad Kandeel, Whitney S. Goldner, Julie Ann Sosa, Gitonga Munene, Venu G. Pillarisetty, Christopher H. Lieu, Boris W. Kuvshinoff, Pamela L. Kunz, Jeffrey F. Moley, Jean Nicolas Vauthey, Thorvardur R. Halfdanarson, Leonard B. Saltz, Jordan Berlin, Paul F. Engstrom, Jennifer L. Burns, Matthew H. Kulke, Emily K. Bergsland, Lyska Emerson, Al B. Benson, Thomas J. Giordano, Lawrence S. Blaszkowsky, Christopher L. Wolfgang, Jonathan R. Strosberg
Rok vydání: 2015
Předmět:
Zdroj: Scopus-Elsevier
ISSN: 1540-1413
1540-1405
DOI: 10.6004/jnccn.2015.0011
Popis: Neuroendocrine tumors (NETs) comprise a broad family of tumors that may or may not be associated with symptoms attributable to hormonal hypersecretion. The NCCN Clinical Practice Guidelines in Oncology for Neuroendocrine Tumors discuss the diagnosis and management of both sporadic and hereditary NETs. This selection from the guidelines focuses on sporadic NETs of the pancreas, gastrointestinal tract, lung, and thymus.
Databáze: OpenAIRE